Inhibition of Novel Reassortant Avian Influenza H7N9 Virus Infection in vitro with Three Antiviral Drugs, Oseltamivir, Peramivir and Favipiravir

2014 ◽  
Vol 23 (6) ◽  
pp. 237-240 ◽  
Author(s):  
Rui-Yuan Cao ◽  
Jun-Hai Xiao ◽  
Bin Cao ◽  
Song Li ◽  
Yohichi Kumaki ◽  
...  

Background: A novel reassortant avian-origin influenza A (H7N9) virus was isolated from respiratory specimens obtained from three patients and was identified as H7N9 in China. Antiviral agents are required to treat patients with avian influenza H7N9 virus infection. Methods: In this study, we assessed the antiviral potential of oseltamivir, peramivir, favipiravir (T-705), amantadine and rimantadine against novel reassortant avian-origin influenza H7N9 virus in vitro. Results: All three avian influenza H7N9 virus strains were sensitive to oseltamivir, peramivir and favipiravir (T-705), but resistant to amantadine and rimantadine. Conclusions: Our data show a pattern of antiviral sensitivity for this novel H7N9 strain of influenza that suggests the compounds oseltamivir, peramivir and favipiravir should be useful for therapy.

Vaccine ◽  
2015 ◽  
Vol 33 (18) ◽  
pp. 2152-2158 ◽  
Author(s):  
Ye V. Liu ◽  
Michael J. Massare ◽  
Melissa B. Pearce ◽  
Xiangjie Sun ◽  
Jessica A. Belser ◽  
...  

2014 ◽  
Vol 20 (2) ◽  
Author(s):  
Xian Qi ◽  
Lunbiao Cui ◽  
Ke Xu ◽  
Bin Wu ◽  
Fenyang Tang ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e77651 ◽  
Author(s):  
Jindong Shi ◽  
Juan Xie ◽  
Zebao He ◽  
Yunwen Hu ◽  
Yanchao He ◽  
...  

2020 ◽  
Vol 80 (3) ◽  
pp. 310-319 ◽  
Author(s):  
Junbo Chen ◽  
Huachen Zhu ◽  
Peter W. Horby ◽  
Qianli Wang ◽  
Jiaxin Zhou ◽  
...  

Viruses ◽  
2014 ◽  
Vol 6 (4) ◽  
pp. 1525-1539 ◽  
Author(s):  
Zheng Zhu ◽  
Yuhua Qi ◽  
Aihua Ge ◽  
Yefei Zhu ◽  
Ke Xu ◽  
...  

2013 ◽  
Vol 66 (6) ◽  
pp. 558-560 ◽  
Author(s):  
Xianfeng Zhou ◽  
Hui Li ◽  
Xiansheng Ni ◽  
Mingbin Liu ◽  
Maohong Hu ◽  
...  

2018 ◽  
Vol 7 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Ming Tan ◽  
Lunbiao Cui ◽  
Xiang Huo ◽  
Ming Xia ◽  
Fengjuan Shi ◽  
...  

Viruses ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1066 ◽  
Author(s):  
Maki Kiso ◽  
Seiya Yamayoshi ◽  
Yuri Furusawa ◽  
Masaki Imai ◽  
Yoshihiro Kawaoka

Viral neuraminidase inhibitors show limited efficacy in mice infected with H7N9 influenza A viruses isolated from humans. Although baloxavir marboxil protected mice from lethal challenge infection with a low pathogenic avian influenza H7N9 virus isolated from a human, its efficacy in mice infected with a recent highly pathogenic version of H7N9 human isolates is unknown. Here, we examined the efficacy of baloxavir marboxil in mice infected with a highly pathogenic human H7N9 virus, A/Guangdong/17SF003/2016. Treatment of infected mice with a single 1.5 mg/kg dose of baloxavir marboxil protected mice from the highly pathogenic human H7N9 virus infection as effectively as oseltamivir treatment at 50 mg/kg twice a day for five days. Daily treatment for five days at 15 or 50 mg/kg of baloxavir marboxil showed superior therapeutic efficacy, largely preventing virus replication in respiratory organs. These results indicate that baloxavir marboxil is a valuable candidate treatment for human patients suffering from highly pathogenic H7N9 virus infection.


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